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  <title>NOPR Community:</title>
  <link rel="alternate" href="http://nopr.niscpr.res.in/handle/123456789/15555" />
  <subtitle />
  <id>http://nopr.niscpr.res.in/handle/123456789/15555</id>
  <updated>2026-09-09T18:34:12Z</updated>
  <dc:date>2026-09-09T18:34:12Z</dc:date>
  <entry>
    <title>Mechanochemical synthesis of nanohydroxyapatite bioceramics</title>
    <link rel="alternate" href="http://nopr.niscpr.res.in/handle/123456789/24723" />
    <author>
      <name>Adzila, Sharifah</name>
    </author>
    <author>
      <name>Sopyan, Iis</name>
    </author>
    <author>
      <name>Yong, Tan Chou</name>
    </author>
    <author>
      <name>Singh, Ramesh</name>
    </author>
    <author>
      <name>Hoong, Wong Yew</name>
    </author>
    <author>
      <name>Purbolaksono, J</name>
    </author>
    <author>
      <name>Hamdi, Mohd.</name>
    </author>
    <id>http://nopr.niscpr.res.in/handle/123456789/24723</id>
    <updated>2013-12-12T16:38:16Z</updated>
    <published>2013-12-01T00:00:00Z</published>
    <summary type="text">Title: Mechanochemical synthesis of nanohydroxyapatite bioceramics
Authors: Adzila, Sharifah; Sopyan, Iis; Yong, Tan Chou; Singh, Ramesh; Hoong, Wong Yew; Purbolaksono, J; Hamdi, Mohd.
Abstract: Nanosized hydroxyapatite powder has been&#xD;
synthesized by the mechanochemical method using a dry mixture of calcium&#xD;
hydroxide and diammonium hydrogen phosphate. The effect of mechanochemical&#xD;
process on powder properties has been investigated. Three rotation speeds of 170&#xD;
rpm, 270 rpm and 370 rpm have been employed with 15 hours milling time.&#xD;
Characterization of the nanopowders has been accomplished by Fourier transform&#xD;
infra red, X-ray diffraction and transmission electron microscopy analyses. The&#xD;
samples have been prepared and sintered in air at varying temperatures ranging&#xD;
from 1050–1350 &lt;span style="font-family:Symbol;mso-ascii-font-family:&#xD;
" times="" new="" roman";mso-hansi-font-family:"times="" roman";mso-char-type:symbol;="" mso-symbol-font-family:symbol"="" lang="EN-GB"&gt;°C. Results show that increase in&#xD;
rotation speed (370 rpm) increases the crystallite size (9–21 nm). Agglomerate&#xD;
formation with irregular shapes is found in the samples prepared at 270 and 370&#xD;
rpm. The sintering process influences the stability of powder by yielding TCP&#xD;
phase at all the sintering temperatures. At 370 rpm, the sample sintered at&#xD;
1250 °C shows the maximum relative density of 95.3% as well as hardness of 5.3&#xD;
GPa.&#xD;
&#xD;
&lt;/span&gt;
Page(s): 1570-1575</summary>
    <dc:date>2013-12-01T00:00:00Z</dc:date>
  </entry>
  <entry>
    <title>Solvent-free synthesis of jasminaldehyde using double metal cyanide based  solid acid catalysts</title>
    <link rel="alternate" href="http://nopr.niscpr.res.in/handle/123456789/24722" />
    <author>
      <name>Patil, Mallikarjun V</name>
    </author>
    <author>
      <name>Sharma, Sumeet K</name>
    </author>
    <author>
      <name>Jasra, Raksh V</name>
    </author>
    <id>http://nopr.niscpr.res.in/handle/123456789/24722</id>
    <updated>2013-12-12T16:38:09Z</updated>
    <published>2013-12-01T00:00:00Z</published>
    <summary type="text">Title: Solvent-free synthesis of jasminaldehyde using double metal cyanide based  solid acid catalysts
Authors: Patil, Mallikarjun V; Sharma, Sumeet K; Jasra, Raksh V
Abstract: The catalytic activity of Fe-Zn double metal&#xD;
cyanide catalysts is studied for the solvent-free synthesis of jasminaldehyde&#xD;
by liquid phase condensation of benzaldehyde and 1-heptanal at 433 K. The&#xD;
highest conversion of 1-heptanal (93%) with 77% selectivity to jasminaldehyde&#xD;
is achieved under the optimum reaction conditions. The presence of&#xD;
co-ordinatively unsaturated Zn&lt;sup&gt;2+ &lt;/sup&gt;in the structural framework of&#xD;
Fe-Zn double metal cyanide assists the condensation reaction. The effects of&#xD;
complexing and co-complexing agent, amount of catalyst, benzaldehyde to&#xD;
1-heptanal molar ratio and temperature on the selectivity of jasminaldehyde is&#xD;
reported.
Page(s): 1564-1569</summary>
    <dc:date>2013-12-01T00:00:00Z</dc:date>
  </entry>
  <entry>
    <title>Facile synthesis of highly dispersed PtSn nanoparticles on carbon nanotubes  with excellent ethanol electrooxidation performance</title>
    <link rel="alternate" href="http://nopr.niscpr.res.in/handle/123456789/24721" />
    <author>
      <name>Wu, Bohua</name>
    </author>
    <author>
      <name>Gong, Ming</name>
    </author>
    <author>
      <name>Chu, Jia</name>
    </author>
    <author>
      <name>Wang, Xiaoqin</name>
    </author>
    <author>
      <name>Xiong, Shanxin</name>
    </author>
    <id>http://nopr.niscpr.res.in/handle/123456789/24721</id>
    <updated>2013-12-19T16:38:46Z</updated>
    <published>2013-12-12T09:44:57Z</published>
    <summary type="text">Title: Facile synthesis of highly dispersed PtSn nanoparticles on carbon nanotubes  with excellent ethanol electrooxidation performance
Authors: Wu, Bohua; Gong, Ming; Chu, Jia; Wang, Xiaoqin; Xiong, Shanxin
Abstract: Stable and&#xD;
uniform PtSn nanoparticles on the surface of carbon nanotubes with ultrafine&#xD;
particle sizes have been prepared via the ionic liquid polymer method.&#xD;
Morphology and electrochemical properties of the PtSn nanoparticles supported&#xD;
on the ionic liquid (IL) polymer-functionalized carbon nanotubes (PtSn/CNTs-f&#xD;
nanohybrids) have been investigated by transmission electron microscopy and&#xD;
cyclic voltammetry. The average diameter of PtSn nanoparticles in &#xD;
the PtSn/CNTs-f nanohybrids is 1.6±0.5 nm, which is much smaller than that&#xD;
deposited on pristine carbon nanotubes (PtSn/CNTs-p nanohybrids, 6±2 nm).&#xD;
The electrochemical active surface area (ESA) of the PtSn/CNTs-f nanohybrids &#xD;
is&#xD;
about twice as high as that of the PtSn/CNTs-p nanohybrids. In comparison to the PtSn/CNTs-p nanohybrids, PtSn/CNTs-f nanohybrids exhibit unexpectedly&#xD;
high activity and stability towards ethanol electrooxidation which may be&#xD;
attributed &#xD;
to the higher dispersion, smaller particle size and higher ESA of the PtSn&#xD;
nanoparticles on the IL polymer functionalized CNTs material. The results&#xD;
indicate that PtSn/CNTs-f nanohybrids are promising anodic electrocatalyst for&#xD;
direct &#xD;
ethanol fuel cells.
Page(s): 1557-1563</summary>
    <dc:date>2013-12-12T09:44:57Z</dc:date>
  </entry>
  <entry>
    <title>Solvothermal synthesis and characterization of zinc sulphide nanoparticles</title>
    <link rel="alternate" href="http://nopr.niscpr.res.in/handle/123456789/24720" />
    <author>
      <name>Mishra, Deepti</name>
    </author>
    <author>
      <name>Prabhakar, Priyanka</name>
    </author>
    <author>
      <name>Lahiri, Swati</name>
    </author>
    <author>
      <name>Amritphale, S S</name>
    </author>
    <author>
      <name>Chandra, Navin</name>
    </author>
    <id>http://nopr.niscpr.res.in/handle/123456789/24720</id>
    <updated>2013-12-23T16:39:28Z</updated>
    <published>2013-12-12T09:43:24Z</published>
    <summary type="text">Title: Solvothermal synthesis and characterization of zinc sulphide nanoparticles
Authors: Mishra, Deepti; Prabhakar, Priyanka; Lahiri, Swati; Amritphale, S S; Chandra, Navin
Abstract: Zinc sulphide nanoparticles have been&#xD;
synthesized by &#xD;
solvothermal approach involving refluxing of an aqueous solution of zinc&#xD;
acetate and sodium sulphide in presence of ethylene &#xD;
glycol and cetyl trimethyl ammonium bromide as surfactant. &#xD;
The nanoparticles have been characterized by X-ray diffraction, Fourier&#xD;
transform infrared spectroscopy, field emission scanning electron microscopy, &lt;span style="mso-bidi-font-weight:bold"&gt;energy-dispersive X-ray spectroscopy, &#xD;
differential scanning calorimetry, thermogravimetric analysis,&#xD;
ultraviolet-visible spectroscopy and transmission electron &#xD;
microscopy. The FESEM results indicate that the particles are almost spherical in shape with size varying in the range of &#xD;
27.7–49.5 nm,&#xD;
whereas TEM micrograph indicates formation of particles&#xD;
of size in the range of 5–8 nm. EDX spectrum reveals the predominance of carbon, zinc, oxygen and&#xD;
sulphur.&#xD;
&#xD;
&lt;/span&gt;
Page(s): 1591-1594</summary>
    <dc:date>2013-12-12T09:43:24Z</dc:date>
  </entry>
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